Abstract
A novel method is described for the one-pot synthesis of various ionic liquids in
a competitive time. By using ultrasonic irradiation, different families of nitrogen-bearing
ionic liquids can be obtained in a solvent-free or in aqueous medium, which gives
a greener touch to the overall process.
Key words
ionic liquids - ultrasound - solvent-free reaction
References and Notes
<A NAME="RG09907ST-1">1 </A> For review on ionic liquids, see:
Welton T.
Chem. Rev.
1999,
99:
2071
<A NAME="RG09907ST-2">2 </A>
Khandekar AC.
Khadilkar BM.
Synlett
2002,
152
<A NAME="RG09907ST-3">3 </A>
Estager J.
Lévêque J.-M.
Turgis R.
Draye M.
J. Mol. Catal. A: Chem.
2006,
256:
261
<A NAME="RG09907ST-4">4 </A>
Price BK.
Hudson JL.
Tour JM.
J. Am. Chem. Soc.
2005,
127:
14867
<A NAME="RG09907ST-5">5 </A>
Zhang S.
Hou Y.
Huang W.
Shan Y.
Electrochim. Acta
2005,
50:
4097
<A NAME="RG09907ST-6">6 </A>
Ranke J.
Müller A.
Bottin-Weber U.
Stock F.
Stolte S.
Arning J.
Störmann R.
Jastorff B.
Ecotoxicol. Environmen. Safety
2007,
in press
<A NAME="RG09907ST-7">7 </A>
Holbrey JD.
Seddon KR.
J. Chem. Soc., Dalton Trans.
1999,
2133
<A NAME="RG09907ST-8">8 </A>
Namboodiri VV.
Varma RS.
Tetrahedron Lett.
2002,
43:
5381
<A NAME="RG09907ST-9">9 </A>
Neppiras EA.
Phys. Rep.
1980,
61:
159
<A NAME="RG09907ST-10">10 </A>
Suslick K.
Schubert P.
Goodale J.
J. Am. Chem. Soc.
1981,
103:
7342
<A NAME="RG09907ST-11">11 </A>
Luche JL. In
Synthetic Organic Sonochemistry
Plenum Press;
New York:
1998.
p.169
<A NAME="RG09907ST-12">12 </A>
Lévêque J.-M.
Luche J.-L.
Pétrier C.
Roux R.
Bonrath W.
Green Chem.
2002,
4:
357
<A NAME="RG09907ST-13">13 </A>
Xu D.-Q.
Liu B.-Y.
Luo S.-P.
Xu Z.-Y.
Shen Y.-C.
Synthesis
2003,
2626
<A NAME="RG09907ST-14">14 </A>
Sonochemistry: Theory, Applications and Uses of Ultrasound in Chemistry
Mason TJ.
Lorimer JP.
Ellis Harwood;
Chichester, UK:
1988.
p.9
<A NAME="RG09907ST-15">15 </A>
The used ultrasonic probe was a Branson 20 kHz digital sonifer or a Ultrasons Annemasse
S.A. 30 kHz probe. Acoustic powers were determined by calorimetry.
[17 ]
1 H and 13 C NMR spectra were recorded on a Bruker AMX 200 MHz spectrometer. IR analyses were
performed on an ATI Mattson Genesis Series FTIR instrument. All precursor products
are commercially available and were used without further purification. Potassium salts
(1 equiv), alkyl bromide (1 equiv) and nitrogen-bearing heterocycles were introduced
in a 25-mL cooling-jacket glass reactor. H2 O was added when 1-bromobutane was used as alkyl bromide. The medium was sonicated
at 20 kHz or 30 kHz for the times and at the temperatures and acoustic powers listed
in Tables
[1 ]
and
[3 ]
-5. A heat-conducting fluid was used in the cooling jacket to maintain the overall
temperature at about 80 °C during the experiments. The final mixture was then poured
into acetone and filtered through Celite. Acetone was removed under vacuum. Hydrophobic
ILs were washed with H2 O (4 × 20 mL) and Et2 O (4 × 20 mL), to be finally dried at 90 °C under vacuum (3 h). Hydrophilic ILs were
dissolved in H2 O (50 mL) and extracted with CH2 Cl2 (4 × 25 mL); solvents were removed under vacuum and RTILs are washed with Et2 O (4 × 20 mL) to be finally dried at 90 °C under vacuum (3 h). All products were checked
by 1 H and 13 C NMR spectroscopy and no organic impurity was observed. No significant trace of H2 O was observed in the IR spectra.
<A NAME="RG09907ST-16">16 </A>
Anastas PT.
Warner JC.
Green Chemistry: Theory and Practice
Oxford University Press;
Oxford:
1998.
p.30
<A NAME="RG09907ST-17">17 </A>
Kimura T.
Sakamoto T.
Lévêque J.-M.
Sohmiya H.
Fujita M.
Ikeda S.
Ando T.
Ultrason. Sonochem.
1996,
3:
S157